sudden death Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Rapid and unexpected death. (Human Phenotype Ontology, HP_0001699)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001699
Similar Terms
Downloads & Tools

Genes

14 genes associated with the sudden death phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CALM1 calmodulin 1 (phosphorylase kinase, delta)
CASQ2 calsequestrin 2 (cardiac muscle)
CAV3 caveolin 3
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
HRAS Harvey rat sarcoma viral oncogene homolog
JUP junction plakoglobin
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYLK2 myosin light chain kinase 2
RYR2 ryanodine receptor 2 (cardiac)
SCN5A sodium channel, voltage gated, type V alpha subunit
SOST sclerostin
TNNT2 troponin T type 2 (cardiac)
TTN titin